149 Sterile Jobs - Page 5

Handling of all Vendor Management related activities including qualification of Vendors, Service Providers, Contract Manufacturing and Contract Testing Laboratories across R&D, API and Formulation units of Biological E, pharma divisions. To perform On-site audits as part of vendor audits, contract testing laboratories, contract manufacturing, external service vendors qualifications. Initiation and Review of Quality Management Systems (QMS), including Change controls, Deviations, Investigation reports and CAPAs. To perform Risk assessments related to Vendor, Contract Testing Laboratories and Contract Manufacturing and Service Provider qualification related activities. Preparation & review of Quality agreements & Technical agreements. To provide support / relevant information to the customers / suppliers as per the requirement and to provide remediation plans for the audit observations, if any To schedule, perform the self-inspections and review the Self-Inspection reports and relevant documents as applicable. To facilitate and review the performance of quality system through the review of QMS documents for Management Review Meetings. To co-ordinate for Management Review Meetings. To review and monitor the effectiveness of system changes and adequacy of CAPAs and post closure effectiveness checks. To track the health authorities observations at the Site and R&D and verify the compliance. To coordinate with the team for preparation and implementation of SOPs pertaining to Corporate Quality.

Department : Production Sciences or Pharmacy Graduates (M.Sc. / B. Pharm. / M. Pharm.) with 1 to 6 years Experiences in parenteral manufacturing (vial / ampoules / bottles of glass or Plastic through BFS technology). Candidate worked in production compliances / remediation / and having experiences of managing quality system document (CCN / CAPA / investigation etc.) Note : We also invite CV for various position in Production, QA, QC, F&D & Maintenance kindly forward the same to E Mail : rajeshthakor@aculife.co.in’

Amneal is coming in your city Hyderabad this 07th & 08th Jun 2025 for Walk In Drive Hiring for Projects & Engineering and Peptide expereince : Walk-In Interview Drive #Hyderabad We are coming to your city for a walk-in interview drive! If you're looking to build a rewarding career with a growing Global Pharmaceutical Company, dont miss this opportunity. Day 1: Saturday, 07th June 2025 Time: 9:00 AM to 5:00 PM Venue: Lemon Tree Premier Plot No. 2, Survey No. 64, HITEC City, Madhapur, Hyderabad 500081, Telangana Day 2: Sunday, 08th June 2025 Time: 9:00 AM to 5:00 PM Venue: Vivanta Hyderabad, Begumpet 1-10-147 & 148, Mayuri Marg, Begumpet, Hyderabad 500016, Telangana Opening in Engineering Department for the following opening : Designation : Sr Executive / Manager Yrs of Exp : 5-12 Yrs Qualification : M.Tech / B.E Expereince into Electrical : Experienced in electrical project execution, compliance, and commissioning, with strong knowledge of HT and LT electrical systems and a solid understanding of pharmaceutical equipment requirements. Expereince into Instrumentation Skilled in automation and instrumentation of equipment and utility systems, with hands-on experience in regulatory compliance, calibration, temperature mapping, and thermal validation. Expereince into Civil Civil engineer overseeing site execution, quality assurance, regulatory compliance, cross-functional coordination, and project documentation in pharmaceutical projects. Expereince into Mechanical Mechanical project scope includes HVAC systems, utility services, regulatory compliance, project timelines, and cross-functional coordination. In-depth knowledge of process equipment used in injectable pharmaceutical plants experience in the installation, commissioning, and qualification of water systems. Expereince into Process Strong expertise in equipment used for injectable manufacturing, with preferable knowledge of isolator systems. Experienced in the installation, commissioning, qualification, and documentation of process equipment Interested candidates who are unable to attend interview, can share their CV on below mentioned Email Id with subject line Application for Falcon indiacareers@amneal.com

Relevant Skills and Responsibilities: Cleaning: CSSD technicians are responsible for thorough cleaning of instruments and equipment. Sterilization Procedures: This encompasses knowledge of various sterilization methods. Inventory Management: CSSD technicians manage the inventory of sterilized instruments and supplies. Documentation: Maintaining accurate records is a key responsibility. Packaging: CSSD technicians are responsible for packaging items for sterilization and storage. Role & responsibilities Preferred candidate profile

Role & responsibilities To Lead QC Function (QC chemical & Micro) of both main QC and DPI QC lab Handle Audit Readiness, Investigation, documents review. Day to day Work allocation and meeting timeline of RM, PM, FG, stability Studies Team Management (QC, Micro) Coordinate with such as WH, Production, QA, PPIC, etc

Role & responsibilities To generate the correct EPLAN drawings. To deliver the correct bill of material and E-plan drawing as per schedule Study & Understand the new project from P&ID and Order Confirmation Interact with customer along with project / sales team to understand the customer needs by visiting customer location Understand scope of the project as per the inputs from Order by participating Kickoff meetings Analyze and extract the required inputs for automation from Engineering department Understand the final process/out come at customer end from Process Engineering department According to inputs prepare electrical drawings by using E-plan software Preferred candidate profile Must have experience of Sterile/ Injectibles/ Biopharma division. Hands on Experience on EPLAN Knowledge of AutoCAD software

Role & responsibilities 1. Study& Understand of Project from P&I Diagram & Functional Specification Document. 2. Development Of Siemens PLC& WinCC SCADA or Rockwell PLC and SCADA. 3. Testing & Deliver PLC & SCADA program with quality & accuracy w.r.t. Functional Specification. 4. Co-ordination across cross fucntional team like QA,Process,Engineering,Factory. 5. Participating project kick-off , Internal FAT & customer FAT. 6. Site visit for commissioning. 7. Compliance of customer queries at the time Of FAT. Preferred candidate profile Must have experience of Sterile/ Injectibles/ Biopharma division.

Walk In Drive For Production Injectables In Formulation Division @ Bollaram Department:- Production Injectables Qualification :-ITI | BA | Diploma | B Com | BSC | B Pharmacy Experience :- 2 To 8 Years Skills :- LYO operator | Packing | Packing (Labelling) | Vial Filling & sealing | Compounding | QMS & Documentations | Autoclave | Aseptic processing area | Vial washing & Tunnel | Filling Division :- Formulation Interview Date:- 08-06-2025 Interview Time :- 9.00AM TO 2.00PM Work Location:- MSNF-II , Kothur | MSNF-V, Rk Puram Venue Location:- Plot No- 42, Anrich Industrial Estate, Bollaram Village, Hyderabad, Telangana 502325 Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Pay slips, Bank Statement, Certificates, Aadhar Card & Pan Card We are looking for candidate those who have experience in Lyo, Compounding, Autoclave,Vial Filling, Vial Washing, Sealing,Aseptic Processing Area, Tunnels, Labelling, About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

Sterile Operations Trainer Grade: G8 Designation: Deputy General Manager Location: Halol 1 Job Description: Education: B. Pharm / M. Pharm Overall responsibility of Aseptic Training Academy (ATA), Baska To plan, develop, and execute training at Aseptic Training Academy (ATA) - Sterile Operations for Sun Global Operations (SGO) Training. Creation of simplified training modules for technicians, scheduling and execution of training Creation of training evaluation and/or feedback systems Course creation according to levels (Level 1 - Technicians, Level 2 - Supervisors and above, Level 3 - Managers and above) pertaining to sterile operations Planning, scheduling & execution of technical training program relevant to sterile operations for new recruits/for existing employee by self/internal or external facility Identification of Certified trainer at various locations (sterile operations) based on additional training need of respective location Coordination with location head and Subject Matter Expert (SME) for conducting the additional training program according to training calendar on monthly basis pertaining to sterile operations To prepare and submit SGO training score card for sterile operations on monthly basis after plant review to Corporate Quality Policy and Training department (CQPT) To maintain the training records of training Periodical review of technical courses along with business units for site specific course and the head of course for suitable course content / design and pedagogy up gradation To coordinate in technical course scheduling and publishing of calendars and facilitate visiting faculty/guest faculty in course delivery Any other work assigned by superiors from time to time

Role & responsibilities: : Sales Management Team/Channel management Customer Relationship Management Market Development Compliance and Reporting Budget and Resource Management Preferred candidate profile: : Leadership: Strong ability to manage, motivate, and develop a team of sales professionals at channel partner's level. Communication Skills: Excellent verbal and written communication skills, with the ability to present to clients and senior management. Industry Knowledge: In-depth knowledge of the pharmaceutical industry, Contrast media portfolio is definitely a value addition. Analytical Skills: Strong ability to analyze sales data, identify trends, and make data-driven decisions. Travel: Willingness to travel frequently within the assigned region Perks and benefits: :

Off Targets is a leader in pharmaceutical innovation, committed to developing advanced therapeutic solutions that address unmet medical needs. We are looking for an experienced and dynamic professional to lead our Formulation Development department, driving the development of cutting-edge injectable drug products. Job Description We are seeking an accomplished R&D leader to head our Injectable Formulation Development function. The ideal candidate will bring deep technical expertise in complex injectable products and a strategic mindset aligned with 505(b)(2) development, regulatory planning, and IP differentiation. Key Responsibilities: Lead end-to-end formulation development of complex injectable drug products (liposomes, emulsions, depot injections, suspensions, etc.). Design and drive a robust R&D pipeline focused on 505(b)(2) opportunities . Provide strategic input into USFDA regulatory planning (CMC sections, QbD, stability). Contribute to patent strategy and product differentiation from early development. Collaborate with analytical, regulatory, IP, and business development functions. Mentor a high-performing R&D team and build scientific leadership. Solve scale-up and technology transfer challenges. Maintain strong compliance with global quality and documentation standards. Key Skills: Injectable Formulation, 505(b)(2), Liposomes, Emulsions, Depot Injections, Formulation R&D, CMC, USFDA, Drug Delivery, Intellectual Property, Team Leadership, Innovation Strategy Desired Candidate Profile: Qualification: Ph.D. / M.Pharm in Pharmaceutics or related field Experience: 15+ years in pharmaceutical R&D with at least 5 years in a strategic leadership role Proven expertise in injectable formulations and 505(b)(2) development Strong knowledge of USFDA CMC expectations, IP evaluation , and regulatory submission processes Excellent leadership, innovation, and cross-functional collaboration skills Perks and benefits Opportunity to lead a key department in a forward-thinking pharmaceutical company. A collaborative and supportive work environment that encourages professional growth and innovation. Competitive salary and benefits package, with opportunities for advancement. Access to state-of-the-art facilities and cutting-edge technology. How to Apply: Interested candidates are invited to submit their resume and a cover letter outlining their experience and qualifications to business@offtargets.com

Job Description We are looking for an experienced and dynamic Team Leader to head our Analytical Research team within the Pharmaceutical R&D division, focused on complex injectable products and 505(b)(2) submissions . This role is ideal for a candidate with a strong background in pharmaceutical R&D , robust team management skills , and deep understanding of injectable formulation analytics . Key Responsibilities Lead and manage the analytical research team supporting complex injectable development. Supervise daily lab operations, resource allocation, and project timelines. Drive method development, validation, and troubleshooting for injectable formulations. Provide scientific leadership and ensure data quality and regulatory compliance. Maintain high team morale and cultivate a positive, collaborative work environment. Guide preparation of analytical documents for regulatory filings (505(b)(2), ANDA, etc.). Impart training, develop team capabilities, and mentor junior scientists. Collaborate closely with formulation, quality, and regulatory teams. Ensure compliance with cGMP, GLP, and internal SOPs. Desired Candidate Profile Qualification: M.Pharm / Ph.D. in Pharmaceutical Sciences, Analytical Chemistry, or related field. Experience: 8+ years in Pharmaceutical R&D , minimum 3 years in a leadership/supervisory role . Hands-on experience in analytical method development for complex injectables (liposomes, suspensions, emulsions, etc.). Sound knowledge of 505(b)(2) regulatory pathway . Strong command of analytical techniques: HPLC, GC, spectroscopy, particle size analysis, etc. Proven track record in team leadership, project coordination , and technical problem-solving . Excellent communication and interpersonal skills. Key Skills Analytical R&D, Complex Injectables, Injectable Formulations, Team Management, 505(b)(2), Method Development, HPLC, GC, Troubleshooting, Pharmaceutical R&D, Training & Mentoring

Process Mechanical, Process Electrical, HVAC, Water System with WFI Knowledge, Utility Electrical (Chiller, DG, Air compressor, Heat pump, Boiler)

Greetings from Immacule Lifescience Pvt. Ltd! We are seeking experienced professionals for multiple positions in our Engineering department at our sterile injectable formulations manufacturing plant located in Nalagarh, Himachal Pradesh. Department : Engineering - Sterile Formulations Experience : 4 - 8 years Qualification : B. Tech (Electrical & Instrumentation) / Diploma (Electrical & Instrumentation) Positions Available: Officer / Executive : Plant Maintenance Engineering Executive / Senior Executive : Engineering QMS (Quality Management System) Officer : Building Management System (BMS) & Environmental Management System (EMS) Key Requirements: For plant Maintenance & QMS Hands-on experience with injectable equipment, including: - Vial Washing Machine - Vial Filling Line - Tunnel - Autoclave - Pre-Filled Syringe (PFS) Machine - Strong understanding of engineering principles and practices in a sterile manufacturing environment. How to Apply: Interested candidates can send their updated resumes to Eswar.reddy@immacule.in

Production : Associate /Senior Associate Qualification : B. Pharmacy / M. Pharmacy Experience : 2 to 6 years Must have Injectable and Regulatory Knowledge in any of these areas: Aseptic processing activity (Vial/PFS), Bulk compounding, sterilization,Vial washing & Depyrogenation,Lyophilization & Terminal sterilization process. Infusion bags processing activities, In-process checks and Line Clearance activities, Handling of shift activities and manpower. Computer Proficiency: TW, Documentum , MES & SAP, GEP

Walk-In Drive Hyderabad | June 1, 2025 Join our growing team at OneSource The new way to CDMO We're hiring for multiple roles across our R&D and Manufacturing facilities in Bengaluru. Walk-In Interview Details: Date: Sunday, June 1, 2025 Time: 9:00 AM 4:00 PM Venue: Oakwood Residence, 115/1, Road No. 2, Financial District, Gachibowli, Hyderabad, Telangana 500032 Open Positions: Process Development Lab (Unit 1, Bommasandra) Research Associate | Sr. Research Associate | Scientist Qualification: B.Tech / M.Tech (Biotechnology) Experience: 2 – 12 years Drug Substance Manufacturing (Unit 2, Doddaballapura) Executive | Sr. Executive Qualification: MSc / B.Tech / M.Tech (Biotech, Microbiology) Experience: 2 – 8 years Drug Product Manufacturing (Unit 2, Doddaballapura) Executive | Sr. Executive | Team Leader Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm Experience: 2 – 12 years in sterile injectables

To provide effective disinfection and sterilization services. Assist in performing sterilization activities, such as reprocessing, segregation, decontamination and packing under supervision of medical and surgical equipment/instruments. Assist in performing sterilization activities, ensures all surgical items and instruments are sterilized as per the rules and with the required procedure. Essential duties and responsibilities Responsible for receipt of different un-sterile instrument packs with a checklist and record in appropriate register. Disassembling, decontaminating, inspecting and reassembling surgical/medical instruments in accordance with established procedures. Responsible for cleaning setting up the sets as per the protocol. Autoclave according to laid down protocol and dispatch to respective departments/sections. Ensure that each autoclave cycle is recorded. Packing and wrapping, sealing and labelling instruments and sets. Contributes to effective communication, facilitating teamwork and co-operation within the Department and with other Departments. Responsible for the care and handling of all surgical instruments, sterile stock, linen, supplies and equipment in line with competencies. Performs all duties in accordance with position description & CSSD Technician Competencies Initiates and maintains effective communication lines and teamwork/collaboration within the Operating Theatre & CSSD Maintains a safe clean environment using only authorized cleaning products and adheres to the principles of infection control Promotes & adheres to Occupational Health & Safety Policies & Procedures Any other tasks assigned by supervisor that you are capable to perform. Participates as a team member promoting and contributing to a supportive team environment Attends all compulsory core education and teamwork within the facility Set up instrument wash room with distinct areas for clean and dirty. Set up of all Sterilizers Apply the principles of microbiology & infection control to all activities in restricted and semi-restricted areas. To maintain Quality Control parameters for all methods of sterilization and to document the effectiveness of each method. Working conditions Will work in Shifts (Morning, Evening & Night) of 8.5 hours a day. Will remain on call for emergencies. Stretched working hours Skills & Abilities Should have very good assisting skill. Should have basic knowledge of computers. Should be polite & good in communication while handling patient. Role & responsibilities Preferred candidate profile Perks and benefits

Role & responsibilities: Perform sterilization of surgical instruments and medical equipment. Operate autoclaves and other sterilization equipment. Ensure compliance with infection control protocols. Maintain and monitor sterilization records and inventory. Assist in the preparation and packing of instruments for surgeries. Preferred candidate profile : Diploma with Minimum 2+ Years experience as CSSD Technician in Hospital For inquiries, kindly reach out to - Mr. Hament, at 7011324972 or via email at hament.gautam@fortishealthcare.com

Job Description Roles & Responsibilities You will be responsible for end to end Formulation development of Injectable including development, execution, filing and approval. You will be responsible to co-ordinate closely with analytical team to devise effective Proof of Concept (POC) for developing generic equivalent of Reference Listed Drug (RLD)/generic Injections. You will be responsible to support in scale-up to pilot/plant scales for Injectable Products. You will be responsible to monitor the development for robust, effective and bioequivalent drug product in timely manner adhering to safety and quality standards. Also provide support in documentation for regulatory submissions. You will be responsible for technology transfer and execution of the batches. You will be responsible for performing pre-formulation studies for material characterization, drug-excipient compatibility and Reference Listed Drug (RLD) characterization (including reverse engineering, formulation designing and optimization, processes designing and scale up). You will be responsible for preparation of risk evaluation and risk mitigation documents, Scale-up batch documents, and filing documents for drug product at every stage of development. You will be responsible to review data generated and participate in discussions with experts to conclude on prototype(s). Participate in strategizing the sourcing of Active Pharmaceutical Ingredient (API), raw materials and ensure development studies are performed related to regulatory and internal system requirements. You will be responsible for designing and implementing stability studies for injectable formulations to ensure product quality and shelf life. You will be accountable for troubleshooting formulation and process-related issues during development and manufacturing stages. You will collaborate with cross-functional teams to ensure alignment of formulation development with regulatory requirements and commercial objectives. You will be responsible for staying current with emerging technologies and regulatory guidelines in injectable drug development and incorporating them into your work. You will mentor junior scientists and contribute to the continuous improvement of the formulation development process. Qualifications Educational qualification: Masters in Pharmaceutical/M.Tech in Chemical Engineering Minimum work experience: 5 to 8 years of experience in pharmaceutical company in Injectable products. Skills & attributes: Technical Skills Have work experience on Formulation Development and expertise in inhalation/injectable dosage form. Experience in areas of product development for Generic Injectable Experience in Quality by Design (QbD). Experience in Process Optimization and scale up. Experience in Operational Excellence. Knowledge on Good Manufacturing Practice and Good Laboratory Practice. Experience in Technology Transfer. Behavioral Skills Excellent communication and interpersonal skills. Strong analytical and problem-solving abilities. Ability to work collaboratively with own team and cross-functional teams.

Responsibilities: It will be 6 days of working Develop injectable formulations within sterile environment Ensure compliance with regulatory standards throughout product lifecycle Collaborate cross-functionally on project delivery

Method development & Validation ( HPLC /GC/ UV/ Potentiometer etc..) for both Solid orals and Injectables & Handling of all analytical instruments/ Equipments, SOPs prepation, SPEC and STPs prepation/ review,Stability samples analysis .

Location: Gandhinagar, Gujarat (On-site) Job Title: Quality Control (QC) Engineer Position Details Department: Quality Control Reporting To: Senior QC Engineer Working Days: 6 days/week Industry Preference (Mandatory) Applicants must have prior work experience in at least one of the following regulated manufacturing sectors: Sterile/Injectables Manufacturing Medical Devices Manufacturing Medicinal Equipment Manufacturing Position Overview We are looking for a proactive and detail-driven Quality Control (QC) Engineer with 3- 5 years of experience in Sterile/Injectables, Medical Devices, or Medicinal Equipment manufacturing environments. This role is critical to ensuring consistent product quality through comprehensive analytical testing and adherence to stringent regulatory standards. The ideal candidate will have hands-on expertise in chemical analysis, pharmacopeial testing, and GMP-compliant documentation, especially within a sterile or cleanroom environment. Key Responsibilities Conduct routine testing of raw materials, in-process samples, and finished products in accordance with pharmacopeial guidelines (IP/BP/USP/Ph. Eur.). Perform detailed Pharma Copea Testing including identification, assay, dissolution, impurity profiling, and other analytical parameters. Execute general wet chemistry procedures along with pH and conductivity testing . Operate and calibrate analytical instruments including IR Spectroscopy , STIR , and related chemical analysis equipment. Ensure strict compliance with Good Manufacturing Practices (GMP) , Good Laboratory Practices (GLP) , and internal Standard Operating Procedures (SOPs) . Maintain complete and accurate documentation including test reports, calibration records, instrument logs, and change control records. Support investigations related to Out of Specification (OOS) and Out of Trend (OOT) results, including root cause analysis and CAPA. Liaise with Quality Assurance (QA) , Production , and R&D teams for resolution of analytical issues and technical support. Prepare for and participate in internal and external audits, ensuring full laboratory compliance and readiness. Manage sample collection, labeling, storage, and contribute to stability studies where applicable. Candidate Requirements Educational Qualification (Preferred): B.Sc / M.Sc in Chemistry B.Pharm / M.Pharm with a focus on Pharmaceutical Chemistry Experience: 3- 5 years of relevant experience in a pharmaceutical or regulated manufacturing environment Must have worked in Sterile , Injectables , Medical Devices , or Medical Equipment manufacturing Technical Skills: In-depth knowledge of pharmacopeial testing methods and documentation practices Hands-on experience with IR Spectroscopy, STIR, pH meters, and conductivity meters Familiarity with analytical method validation and instrument calibration Strong understanding of Data Integrity , GDP (Good Documentation Practices) , and compliance in regulated cleanroom settings

Kamla Homes is looking for Officer - Sterile Ointment to join our dynamic team and embark on a rewarding career journey Oversee sterile ointment production in cleanroom settings Monitor batch records and ensure GMP compliance Perform in-process checks and manage documentation Ensure safety and quality in operations

Greetings From SP Accure Labs!!! We are conducting Walk-In Interview for Production Injectables formulation department for Compounding Chemist on 30/05/2025 Friday @ our Shamirpet Plant facility. Roles and Responsibilities Conduct quality control tests on injectable products using techniques such as SIP, CIP, TOFFLON, PFS, ISOLATORS, LYOPHILIZATION. Ensure compliance with cGMP guidelines during production activities. Department - Production Role - Compounding activities like CIP, SIP Mixing & Filling Vessels. Desired Candidate Profile 4-8 years of experience in a similar role with (M.Pharmacy, M.Sc, B.Pharma / B.Sc). Strong understanding of chemistry principles applied to pharmaceuticals. Proficiency in compounding, parenteral production, sterile processing, and lyophilization techniques. Experience working with injectable products including oncology treatments. Thanks & Regards, Archana Reddy Team HR

Inspection and verification of In-process activity in Manufacturing Area. Monitoring of Handover Activity of ARM/Bulk. Verification of Packing and Dispatch activity for Final ARM/Bulk. Issuance of Cell Bank / Issuance of Reference standard.